Canonical Allele Identifier: CA370636741
Gene: NAT2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.18258355C>A (hg19) chr8:g.18400845C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18400845C>A , CM000670.2:g.18400845C>A GRCh38
NC_000008.10:g.18258355C>A , CM000670.1:g.18258355C>A GRCh37
NC_000008.9:g.18302635C>A NCBI36
NG_012246.1:g.14601C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000286479.4:c.842C>A MANE Select ENSP00000286479.3:p.Pro281His
ENST00000286479.3:c.842C>A ENSP00000286479.3:p.Pro281His
ENST00000520116.1:c.452C>A ENSP00000428416.1:p.Pro151His
NM_000015.2:c.842C>A NP_000006.2:p.Pro281His
XM_011544358.1:c.842C>A XP_011542660.1:p.Pro281His
XM_017012938.1:c.842C>A XP_016868427.1:p.Pro281His
NM_000015.3:c.842C>A MANE Select NP_000006.2:p.Pro281His
Search 100 bp 5'
Search 100 bp 3'